- PRECAUTIONS
- INDICATIONS:
-
DOSAGE & ADMINISTRATION
DOSAGE AND ADMINISTRATION: May be injected intravenously, subcutaneously or intraperitoneally (except in horses) using strict aseptic technique.
Cattle and Horses: 2 to 5 mL per pound of body weight depending on size and condition of animal, repeated 1 to 3 times daily or as needed.
Swine and Sheep: 2 to 5 mL per pound of body weight depending on size and condition of animal, repeated 1 to 3 times daily or as needed.
If administered subcutaneously divide the dosage into several sites of injection and massage points of injection to aid in absorption and help prevent inflammation and/or sloughing.
- STORAGE AND HANDLING
-
DOSAGE FORMS & STRENGTHS
EACH 100 mL CONTAINS:
Sodium Chloride....................600 mg
Sodium Lactate.....................310 mg
Potassium Chloride.................30 mg
Calcium Chloride Dihydrate......20 mg
Water for Injection.......................q.s.
The Calcium, Potassium and Sodium contents are approximately 2.7, 4.0 and 130 mEq/liter, respectively. Total Osmolar Concentration: 269 mOsmol per liter (calculated).
- PRECAUTIONS
- WARNINGS
- INFORMATION FOR OWNERS/CAREGIVERS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LACTATED RINGERS
lactated ringers injection, solutionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:57699-803 Route of Administration INTRAVENOUS, SUBCUTANEOUS, INTRAPERITONEAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium Chloride (UNII: 451W47IQ8X) (Sodium Cation - UNII:LYR4M0NH37) Sodium Chloride 600 mg in 1000 mL Sodium Lactate (UNII: TU7HW0W0QT) (Sodium Cation - UNII:LYR4M0NH37) Sodium Lactate 310 mg in 1000 mL Potassium Chloride (UNII: 660YQ98I10) (Potassium Cation - UNII:295O53K152) Potassium Chloride 30 mg in 1000 mL Calcium Chloride (UNII: M4I0D6VV5M) (Calcium Cation - UNII:2M83C4R6ZB) Calcium Chloride 20 mg in 1000 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57699-803-60 1000 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/25/2013 Labeler - A & G Pharmaceuticals, Inc. (182147033) Registrant - A & G Pharmaceuticals, Inc. (182147033) Establishment Name Address ID/FEI Business Operations Nova-Tech Inc. 196078976 manufacture Establishment Name Address ID/FEI Business Operations K+S KALI GmbH 507531213 api manufacture